The “microcephalic hydrocephalus” paradox as a paradigm of altered neural stem cell biology

Author:

Duy Phan Q12ORCID,Mehta Neel H3ORCID,Kahle Kristopher T345ORCID

Affiliation:

1. University of Virginia School of Medicine Department of Neurosurgery, , Charlottesville, VA 22908, United States

2. University of Virginia School of Medicine Department of Neuroscience, , Charlottesville, VA 22908, United States

3. Massachusetts General Hospital Department of Neurosurgery, , Boston, MA 02114, United States

4. Broad Institute of MIT and Harvard , Cambridge, MA 02142, United States

5. Massachusetts General Hospital Harvard Center for Hydrocephalus and Neurodevelopmental Disorders, , Boston, MA 02114, United States

Abstract

Abstract Characterized by enlarged brain ventricles, hydrocephalus is a common neurological disorder classically attributed to a primary defect in cerebrospinal fluid (CSF) homeostasis. Microcephaly (“small head”) and hydrocephalus are typically viewed as two mutually exclusive phenomenon, since hydrocephalus is thought of as a fluid “plumbing” disorder leading to CSF accumulation, ventricular dilatation, and resultant macrocephaly. However, some cases of hydrocephalus can be associated with microcephaly. Recent work in the genomics of congenital hydrocephalus (CH) and an improved understanding of the tropism of certain viruses such as Zika and cytomegalovirus are beginning to shed light into the paradox “microcephalic hydrocephalus” by defining prenatal neural stem cells (NSC) as the spatiotemporal “scene of the crime.” In some forms of CH and viral brain infections, impaired fetal NSC proliferation leads to decreased neurogenesis, cortical hypoplasia and impaired biomechanical interactions at the CSF–brain interface that collectively engender ventriculomegaly despite an overall and often striking decrease in head circumference. The coexistence of microcephaly and hydrocephalus suggests that these two phenotypes may overlap more than previously appreciated. Continued study of both conditions may be unexpectedly fertile ground for providing new insights into human NSC biology and our understanding of neurodevelopmental disorders.

Funder

National Institute of Neurological Disorders and Stroke

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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